Computer Science
Scientific paper
Dec 1994
adsabs.harvard.edu/cgi-bin/nph-data_query?bibcode=1994e%26psl.128..407l&link_type=abstract
Earth and Planetary Science Letters (ISSN 0012-821X), vol. 128, no. 3-4, p. 407-423
Computer Science
40
Basalt, Electron Probes, Mass Spectroscopy, Melts (Crystal Growth), Uranium, Chemical Composition, Thermopiles
Scientific paper
The partitioning of U, Th, Pb, Sr, Zr and Ba between coexisting chromian diopsides and haplobasaltic liquids at oxygen fugacities between the iron-wustite buffer and air at 1285 C has been characterized using secondary ion mass spectrometry. The partition coefficients for Th, U and Zr show a strong dependence on the Al and Na content of the clinopyroxene. A good correlation between Al-IV and DTh exists for all recent Th partitioning studies, providing a simple explanation for the two order of magnitude variation in DTh observed in this and previous studies. Because mantle clinopyroxenes generally have greater than 5 wt% Al2O3, we suggest that the relevant partition coefficients for U and Th are between 0.01 and 0.02. While variations in Al and Na in clinopyroxene affect the absolute value of the Th and U partition coefficients, they have no effect on their ratio, DTh/DU. Our results reinforce the inference that equilibrium partioning of U and Th between clinopyroxene and melt cannot explain the observed Th-230 excesses in basalts. Indeed, under the oxygen fugacities relevant to mid-ocean ridge basalts (MORB) petrogenesis, clinopyroxene has little ability to fractionate U from Th (DTh/D(sub U less than 2), implying that chemical disequilibrium between melt and wall rock during transport is not required to preserve Th-230 excess generated in the garnet stability field. If the Ba partition coefficient serves as an analog for Ra and the partition coefficient of U(5+) serves as an analog for Pa(5+), then Ra-226 and Pa-231 excesses can be generated by clinopyroxene-melt partitioning. Using compositionally dependent partition coefficients, a melting model is used to show that equilibrium porous flow can explain variation in uranium series activities from the East Pacific Rise by varying the depth of melting.
Gill James B.
Lundstrom Craig
Phinney Douglas L.
Ryerson Frederick J.
Shaw Henry F.
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